Maintenance of multipotency and how cells exit this state to adopt a specific fate are central questions in stem cell biology. During vertebrate development, multipotent cells of the dorsal somite, the dermomyotome, give rise to different lineages such as vascular smooth and skeletal muscle, regulated by the transcription factors Foxc2 and Pax3, respectively. Here we show reciprocal inhibition between Pax3 and Foxc2 in the mouse embryo. Using both genetic approaches and manipulation of external signals in somite explants, we demonstrate that the Pax3:Foxc2 ratio modulates myogenic versus vascular cell fates. This provides insight into how cell fate choices are orchestrated by these lineage genes in the dermomyotome.
Pax3:Foxc2 reciprocal repression in the somite modulates muscular versus vascular cell fate choice in multipotent progenitors
Lagha, M.; Brunelli, S.; Messina, G.; Cumano, A.; Kume, T.; Relaix, F.; Buckingham, M. E.
2009-12 / vol 17 / pages 892-9
10.1016/j.devcel.2009.10.021 S1534-5807(09)00444-4 [pii]
1878-1551 (Electronic) 1534-5807 (Linking)
IGMM team(s) involved in this publication
Transcription and Development
Animals; Mice; Cell Differentiation; Embryo, Mammalian/*cytology; Forkhead Transcription Factors/*metabolism; Multipotent Stem Cells/*cytology; Muscle, Skeletal/cytology/*embryology; Muscle, Smooth, Vascular/cytology/*embryology; Paired Box Transcription Factors/*metabolism; PAX7 Transcription Factor/metabolism; Somites/*cytology/metabolism